Canonical Allele Identifier: PA2826133325
Gene: CBS HGNC NCBI

Linked Data

ClinVar Variation Id: 340091

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171480.1:p.Leu101Val
CA10653007
NM_001178009.3:c.301C>G
CA2579808301
NM_001178009.3:c.301_303delinsGTT